Evaluation of stress response in black-tailed prairie dogs (Cynomys ludovicianus) in arid regions from colonies in Chihuahua Mexico.

Among all the regulatory homeostatic networks in vertebrates, the activation of the hypothalamic-pituitaryadrenal axis during the stress response, has gained considerable attention, and the measurement of fecal glucocorticoids (FGC) has become an invaluable tool to assess adrenocortical activity related to stressful events in wild and captive animals. However, the use of FGC requires the validation of measurement techniques and the proper selection of the specific hormone according to the study species. The main objective of this study was to identify the dominant glucocorticoid (GC) hormone in the stress response of black-tailed prairie dogs (Cynomys ludovicianus) in an arid grassland of Chihuahua, Mexico. A capture stress challenge in the field was developed to determine if the levels of glucocorticoids (cortisol and corticosterone) both in serum and fecal samples could be attributed to stress in Cynomys ludovicianus. The samples were analysed with the technique of liquid phase radioimmunoassay , and this study showed that both cortisol and corticosterone are present at measurable levels in serum and fecal samples of black-tailed prairie dogs. We found that both GCs were present in similar concentrations in serum, however, corticosterone concentration in fecal samples was higher than cortisol. Likewise, biochemical validations performed in this study to test the assay reached acceptable levels of reliability. Therefore, we confirm that fecal analysis can be implemented as a method to measure stress responses in wild prairie dogs.

Field immobilization of pygmy spotted skunks from Mexico.

We immobilized 21 pygmy spotted skunks (Spilogale pygmaea), in the tropical deciduous forest at the Chamela Biological Station (Mexico) from October 1994 to May 1997, with a mixture of ketamine (KH) and xylazine (XH). Skunks were immobilized with a mean (+/- SD) dosage of 15.7 +/- 8.3 mg/kg KH and 8.1 +/- 4.3 mg/kg XH. Mean induction and recovery time (n = 21) were 1.7 +/- 1.6 and 34.2 +/- 12.2 min, respectively. One individual was immobilized with XH, induction time was 1 min, and recovery time was 45 min. Foaming salivation was observed in this animal. No other adverse effects were observed for the other animals in this sample.